Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 8:19954240 (forward strand) | View in location tab

Co-located

with COSMIC COSM1097856 (T/A) ; HGMD-PUBLIC CM910262

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16461

This variation has 3 HGVS names - click the plus to show

Variation displays